A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3512955



Internal ID18811236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120368253..120423317hg38UCSC Ensembl
Innerchr11:120238962..120294026hg19UCSC Ensembl
Innerchr11:119744172..119799236hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3855065
hg1955065
hg1855065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046430
Supporting Variants
Samples
Known GenesARHGEF12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3512955
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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